Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1230668019 | Fletcher trait | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 786603018 | Prekallikrein deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 81593014 | Prekallikrein deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 81594015 | Fletcher factor deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Prekallikrein deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Prekallikrein deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Prekallikrein deficiency | Is a | Contact factor deficiency | true | Inferred relationship | Some | ||
| Prekallikrein deficiency | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| Prekallikrein deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Prekallikrein deficiency | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Prekallikrein deficiency | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acquired prekallikrein deficiency | Is a | True | Prekallikrein deficiency | Inferred relationship | Some | |
| Hereditary congenital prekallikrein deficiency | Is a | True | Prekallikrein deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR